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Large Molecular Lab Scientist Ii

Novotech
NovoTech
3+ years
Not Disclosed
10 Jan. 22, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Large Molecular Lab Scientist II

Location: Taipei (Nangang District), Taiwan
Employment Type: Full-Time
Job ID: 3670
Industry: Clinical Research | Biotechnology | Central Laboratory
Posting Date: January 20, 2026

About the Company

Novotech is a global full-service Contract Research Organization (CRO) headquartered in Sydney, Australia, with operations across Asia-Pacific, North America, and Europe. With more than 3,000 employees, 34 offices, and 5,000+ site partnerships, Novotech delivers end-to-end clinical development services across all phases and therapeutic areas. The organization is ISO 27001 and ISO 9001 certified, ensuring the highest standards of data security, quality management, and regulatory compliance.

Position Overview

Novotech is seeking a highly motivated Large Molecular Lab Scientist II to support analytical and laboratory operations within its Central Laboratory services in Taiwan. This role involves hands-on laboratory analysis, documentation, system ownership responsibilities, and participation in regulated environments including GLP, GCP, and CAP. The position is ideal for experienced laboratory professionals with strong technical expertise in molecular or biochemical analysis and familiarity with regulated clinical research environments.

Key Responsibilities

  • Perform laboratory analysis in accordance with approved SOPs, protocols, and regulatory guidance.

  • Draft, review, and approve controlled documents including SOPs, protocols, analytical results, validation records, and study reports.

  • Support laboratory logistics and operations including procurement, inventory management, payment processing, and general laboratory administration.

  • Manage laboratory instruments including maintenance scheduling, calibration coordination, and workspace upkeep.

  • Act as system owner for assigned computerized systems, including validation testing, periodic reviews, and system documentation.

  • Participate in CAP, GCP, GLP, and regulatory compliance training programs.

  • Support sample collection kit preparation, labeling activities, and analytical study project coordination.

  • Contribute to GLP study activities as assigned, in alignment with study-based responsibilities.

  • Provide additional laboratory or project support as delegated by the line manager.

Required Qualifications

Education:

  • Bachelor of Science (4-year degree) in Biochemistry, Biotechnology, Chemistry, Laboratory Science, or a related discipline.

  • Advanced degree preferred for Associate Researcher or Senior Researcher levels.

Experience:

  • Minimum 3 years of hands-on laboratory experience in a regulated laboratory environment preferred.

  • Junior candidates with strong technical competence and relevant laboratory exposure may be considered.

Certifications & Licensure:

  • Medical Technician License required for Associate Researcher or Senior Researcher roles within Central Lab functions.

Knowledge, Skills, and Competencies

  • Strong understanding of laboratory operations and analytical workflows.

  • Working knowledge of CAP, GCP, GLP, and applicable local and international regulatory requirements.

  • Experience with documentation control, system validation, and compliance-driven laboratory environments.

  • Proficiency in written and verbal English; additional language skills are an advantage.

  • Strong problem-solving, time management, and prioritization skills.

  • Ability to work independently and collaboratively within cross-functional clinical research teams.

Why Join Novotech

Novotech offers a collaborative, inclusive, and growth-oriented work environment. Employees benefit from flexible working arrangements, wellness initiatives, paid parental leave, continuous learning programs, and strong leadership support. The organization is committed to diversity, equity, and inclusion, welcoming professionals from all backgrounds including individuals with disabilities, caring responsibilities, and those identifying as LGBTIQ+.

As a Circle Back Initiative Employer, Novotech is committed to responding to every applicant.

Application Process

Interested candidates are encouraged to apply with an updated CV highlighting laboratory experience, regulatory exposure, and technical expertise in molecular or biochemical analysis. Applications are reviewed on a rolling basis.